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WO2011118918A2 - Chaussette de stimulation par micro-courant - Google Patents

Chaussette de stimulation par micro-courant Download PDF

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Publication number
WO2011118918A2
WO2011118918A2 PCT/KR2011/001342 KR2011001342W WO2011118918A2 WO 2011118918 A2 WO2011118918 A2 WO 2011118918A2 KR 2011001342 W KR2011001342 W KR 2011001342W WO 2011118918 A2 WO2011118918 A2 WO 2011118918A2
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WO
WIPO (PCT)
Prior art keywords
microcurrent
control signal
generator
level
human body
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/KR2011/001342
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English (en)
Korean (ko)
Other versions
WO2011118918A3 (fr
Inventor
이지훈
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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Filing date
Publication date
Priority claimed from KR1020100027302A external-priority patent/KR100994208B1/ko
Application filed by Individual filed Critical Individual
Publication of WO2011118918A2 publication Critical patent/WO2011118918A2/fr
Publication of WO2011118918A3 publication Critical patent/WO2011118918A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/18—Applying electric currents by contact electrodes
    • A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/322—Electromedical brushes, combs, massage devices
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/02—Details
    • A61N1/04—Electrodes
    • A61N1/0404—Electrodes for external use
    • A61N1/0408—Use-related aspects
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/02—Details
    • A61N1/04—Electrodes
    • A61N1/0404—Electrodes for external use
    • A61N1/0472—Structure-related aspects
    • A61N1/048—Electrodes characterised by a specific connection between lead and electrode
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/02—Details
    • A61N1/04—Electrodes
    • A61N1/0404—Electrodes for external use
    • A61N1/0472—Structure-related aspects
    • A61N1/0484—Garment electrodes worn by the patient
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/18—Applying electric currents by contact electrodes
    • A61N1/20—Applying electric currents by contact electrodes continuous direct currents
    • A61N1/26—Electromedical brushes; Electromedical massage devices ; Combs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/18—Applying electric currents by contact electrodes
    • A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36—Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/36014—External stimulators, e.g. with patch electrodes
    • A61N1/3603—Control systems
    • A61N1/36034—Control systems specified by the stimulation parameters
    • A—HUMAN NECESSITIES
    • A41—WEARING APPAREL
    • A41B—SHIRTS; UNDERWEAR; BABY LINEN; HANDKERCHIEFS
    • A41B11/00—Hosiery; Panti-hose
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/6802—Sensor mounted on worn items
    • A61B5/6804—Garments; Clothes
    • A61B5/6807—Footwear
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/10—Characteristics of apparatus not provided for in the preceding codes with further special therapeutic means, e.g. electrotherapy, magneto therapy or radiation therapy, chromo therapy, infrared or ultraviolet therapy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/16—Physical interface with patient
    • A61H2201/1602—Physical interface with patient kind of interface, e.g. head rest, knee support or lumbar support
    • A61H2201/165—Wearable interfaces
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2205/00—Devices for specific parts of the body
    • A61H2205/12—Feet
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/02—Details
    • A61N1/04—Electrodes
    • A61N1/0404—Electrodes for external use
    • A61N1/0408—Use-related aspects
    • A61N1/0452—Specially adapted for transcutaneous muscle stimulation [TMS]

Definitions

  • the present invention relates to a sock worn on the foot of the human body to be used for treatment or massage purposes, and more particularly, microcurrent stimulation that can increase the effect of massage or treatment by stimulating by delivering a microcurrent to the foot of the human body. It is about dragon socks.
  • the foot is the body part located at the end of the leg, which is a delicate human organ with 26 bones, 39 joints, 38 muscles, 107 ligaments, and many other capillaries and autonomic nerves. These feet have two pulses, one on the instep and one on the Achilles tendon, and acupuncture points that cover 63 parts of the human body. In addition, the foot is a very important role and function of the human body, such as maintaining the balance of the body, weight support, shock absorption, movement.
  • the most important function of the foot function is the walking function, the pump function of the foot.
  • the pump function of the foot is to help the heart to promote blood circulation and metabolism. Since the position of the heart is higher from the ground since humans start walking upright, the blood circulation becomes more difficult as the blood circulation becomes more difficult. Pump function should be smooth. Thus, the foot is also referred to as the second heart function.
  • Diabetes is known to be caused by changes in diet, bad drinking culture, and lack of exercise caused by modern people's busy schedules.
  • the appearance of diabetes initially causes problems throughout the body, but gradually causes nerves, blood vessels, and the immune system to break down, the nerves are gradually destroyed and blood vessels become clogged, causing the most serious problems in the foot at the end of the body.
  • 15-20% of patients hospitalized with diabetes may show foot ulcers. Foot ulcers are a major obstacle in diabetics, ranging from 28% to amputation, which is astronomical.
  • Diabetic foot disease which is caused by a combination of microvascular disorders, free radicals and glycation of proteins due to prolonged hyperglycemia, includes abnormalities, necrosis, calluses, and refractory athlete's foot. If you have diabetes, your feet will be easily injured. If you are infected with a wound, you will not be treated well, unlike a healthy person, and will gradually spread to the upper part.If you miss the initial treatment period, the disease will progress rapidly and irreversibly. Can cause. In addition, as diabetes progresses, most patients have neuropathy, which is a symptom of sensory neuropathy at the extremities of the lower extremities, resulting in cold, numb, and burning symptoms.
  • the present invention has been made in view of the above point, by being worn on the foot of the human body to deliver a microcurrent to the toes, soles, insteps, ankles, etc. can effectively achieve the foot massage effect or the treatment effect of diabetes mellitus
  • the purpose is to provide a sock for the current stimulation.
  • a microcurrent stimulator formed on at least a portion of the sock and made of conductive yarns
  • a microcurrent generator attached to an upper portion of the ankle part and generating a microcurrent to be applied to a conductive yarn constituting the microcurrent stimulation portion, and applying the microcurrent at a predetermined period during an enable time;
  • connection part formed of the same material as the microcurrent stimulation part to electrically connect the microcurrent stimulation part and the microcurrent generator
  • It includes; the base portion formed of a general yarn on the remaining portion except the microcurrent stimulation portion and the connection portion.
  • the microcurrent generator is attached to a predetermined portion of the ankle top of the microcurrent stimulation socks, a button attachment method that performs the attachment and application of microcurrent simultaneously using a snap fastener of conductive metal material, velcro (velcro) Velcro attachment method using a), having a length adjustable band to the microcurrent generator and can be attached to the microcurrent stimulating socks by any one method selected from the band attachment method worn on the ankle or calf.
  • a pocket portion for accommodating the microcurrent generator, a pair of first connection terminal is formed in the microcurrent generator, a pair of second connection terminal is connected to the connection portion in the pocket portion And the first and second connection terminals are electrically connected as the microcurrent generator is accommodated in the pocket part.
  • the cover part is formed to be openable and closeable on the upper side of the pocket part, and an inner side surface of the cover part and an outer side surface of the pocket part are provided with corresponding coupling means.
  • a power supply unit having a power supply switch for supplying power to the microcurrent generator
  • the microcurrent is generated by using the power supplied through the power supply unit, and the generation period of the microcurrent is controlled using the frequency generated by the frequency generator, and in response to the enable signal input from the outside.
  • a generation current level control unit for adjusting the microcurrent generated in the control chip to a desired level.
  • An embodiment of the microcurrent generator may further include a generation voltage level control unit for controlling the output voltage generated by the control chip to a desired final voltage.
  • a booster boosting a power supply voltage to a boosted voltage of a predetermined level in response to the third control signal of the control unit;
  • a microcurrent having a desired level is generated and supplied to a specific part of the human body through connection terminals connected to the human body, and when the first control signal is input, And a microcurrent output unit for supplying the microcurrent having a phase and supplying the microcurrent having a negative phase when the second control signal is input.
  • the microcurrent output unit includes at least one voltage distribution circuit and a plurality of switching elements, and each of the plurality of switching elements performs a switching operation in response to the first control signal or the second control signal. .
  • the microcurrent output unit generates and supplies a supply level confirmation signal for confirming a human supply level of the microcurrent supplied to the human body, and provides the control unit, and the control unit generates a boosted voltage in response to the supply level confirmation signal. Characterized by controlling the level.
  • the first control signal and the second control signal is a pulse signal having a predetermined period and a certain duty ratio, characterized in that the first control signal and the second control signal has a predetermined phase difference.
  • the control unit may determine whether the human body connection terminals are actually connected to the human body through the supply level confirmation signal, and control whether microcurrent is generated.
  • the microcurrent is transmitted through the microcurrent stimulus formed on the toe, the sole, the instep, the ankle, and the like to be worn on the foot of the human body, so that the massage effect or the treatment effect of diabetes can be more effectively implemented.
  • FIG. 1 is a view showing a sock for microcurrent stimulation according to a first embodiment of the present invention.
  • FIG. 2 is a view showing a sock for microcurrent stimulation according to a second embodiment of the present invention.
  • FIG. 3 is an exploded perspective view showing a sock for microcurrent stimulation according to a third embodiment of the present invention.
  • Figure 4 is a side view showing a sock for microcurrent stimulation according to a third embodiment of the present invention.
  • FIG. 5 is a cross-sectional view taken along the line A-A of FIG. 4.
  • FIG. 6 is a cross-sectional view showing a sock for microcurrent stimulation according to a fourth embodiment of the present invention.
  • FIG. 7 is a cross-sectional view showing a sock for microcurrent stimulation according to a fifth embodiment of the present invention.
  • FIG. 8 is a circuit diagram of a microcurrent generator according to a first embodiment applied to a sock for microcurrent stimulation of the present invention.
  • FIG. 9 is a block diagram showing a microcurrent generator according to a second embodiment applied to a sock for microcurrent stimulation of the present invention.
  • FIG. 10 is a circuit diagram of an example of the microcurrent generator of FIG. 9.
  • FIG. 11 is an operation timing diagram of FIG. 10.
  • FIG. 12 illustrates another embodiment of the boosting unit of FIG. 9.
  • FIG. 1 illustrates a microcurrent stimulating sock 100 according to a first embodiment of the present invention.
  • the microcurrent stimulation socks 100 is a microcurrent stimulation unit (120a, 120b, 120c, 120d), which is formed of a good conductive yarn, the general yarn The base 110 is formed, and the microcurrent generator 150 is formed.
  • the microcurrent stimulation part 120a, 120b, 120c, 120d is selected from at least one selected from the toe part 120a, the ankle part 120c, the instep part 120d, and the sole part 120b of the microcurrent stimulating sock.
  • the portion may be formed by knitting or the like by a conductive yarn of a conductive material.
  • a conductive yarn may be made of a highly conductive thread such as gold sand, silver, or a verb.
  • the ankle portion 120c of the microcurrent stimulation portions 120a, 120b, 120c, and 120d may be formed in a round shape to surround the acupoints behind the ankle or wrap the back portion only at the peach bone portion.
  • the toe portion 120a is formed to cover the entire toe
  • the instep portion 120d and the sole portion 120b are formed to cover the acupoints of the instep and the sole of the foot.
  • the connecting portions 120e and 120f are connected to the microcurrent magnetic pole portions 120a, 120b, 120c and 120d, and the connecting portions 120e and 120f are formed by conductive yarns.
  • the microcurrent stimulation parts 120a, 120b, 120c, and 120d are electrically connected to the microcurrent generator 150 through the connection parts 120e and 120f.
  • the connection part 120e electrically connects the ankle part 120c and the remaining parts 120a, 120b, and 120d of the microcurrent stimulation part 120a, 120b, 120c, and 120d, and the connection part 120f is a microcurrent stimulation part (
  • the ankle portion 120c of the 120a, 120b, 120c, and 120d and the microcurrent generator 150 are electrically connected to each other.
  • connection parts 120e and 120f are formed to be narrow and long and are electrically connected to the terminals of the microcurrent generator 150, respectively.
  • connection part 120f is illustrated only on the front side in the drawing, the same structure is also formed on the back side so that the front and back connection parts 120f are electrically connected to each other to apply a microcurrent, or the microcurrent generators 150 are separated from each other. ) Terminals can be electrically connected.
  • the microcurrent magnetic pole portions 120a, 120b, 120c, and 120d and the connecting portions 120e and 120f may be formed of only conductive yarns, or may be formed by mixing conductive yarns with ordinary yarns. In the case of forming a mixture of conductive yarns and ordinary yarns, the mixing ratio may be appropriately determined to have an optimum effect through various experiments.
  • All of the conduction conductors constituting the microcurrent magnetic pole portions 120a, 120b, 120c, and 120d and the connection portions 120e and 120f should be electrically connected to each other.
  • the base 110 is the remaining portion except for the microcurrent stimulation part 120a, 120b, 120c, 120d and the connection part 120e, 120f of the microcurrent stimulation socks 100, the base part 110 is a general yarn It is formed by knitting. Ordinary yarns are used for the manufacture of socks, yarns well known to those skilled in the art to which the present invention pertains may be used.
  • the microcurrent generator 150 is configured to be detachably attached to an upper side of the ankle portion, and generates a microcurrent of 0 to 1000 mA (not including 0) to generate a microcurrent stimulation part 120a, 120b, or 120c. 120d) and the micro-currents are applied to the connection portions 120e and 120f at regular intervals during the enable time.
  • the microcurrent generator 150 is attached to the upper part of the ankle in order to reduce the discomfort when the user wears as a sock in everyday life, the shape of the part touching the leg can also be rounded to minimize the inconvenience.
  • the attachment portion for attaching the microcurrent generator 150 to the sock is a Velcro attachment method for attaching and attaching a velcro to the sock 100 and the microcurrent generator 150, respectively, or a snap button attached to the sock and the microcurrent generator. (snap fastener) is a button that can be fixed by inserting.
  • the band method can be worn on the ankle or calf. In this case, the length of the band can be in the form of a velcro, a ring, a buckle, and the like.
  • connection portion 120f and the microcurrent generator 150 that transfer the microcurrent supplied from the microcurrent generator 150 to the microcurrent stimulation units 120a, 120b, 120c, and 120d are microcurrent generators 150.
  • the button is made of a conductor such as metal, and the attachment portion of the sock 100 is knitted with a conductive yarn so as to have a function of a connection portion that flows a microcurrent to the sock at the same time.
  • one of the buttons connects the positive electrode and one of the negative poles so that the positive and negative poles of the microcurrent can be differently connected as necessary.
  • a method of connecting the metal terminal attached to the conductive yarn portion of the socks by extracting the positive and negative wires from the microcurrent generator 150 may be used.
  • a metallic material made of a material resistant to corrosion or rust such as copper.
  • FIG. 2 illustrates a microcurrent stimulating sock 100a according to a second embodiment of the present invention.
  • the microcurrent stimulation sock 100a according to the second embodiment of the present invention includes a microcurrent stimulation part 130 that occupies the entire ankle or less of the sock and a base portion 140 positioned at the top of the ankle.
  • the microcurrent stimulation unit 130 may be formed by knitting a conductive yarn and a general yarn as shown in FIG.
  • the microcurrent generator 150 may be detachably attached to the upper portion of the ankle, and a connecting portion electrically connecting the microcurrent generator 150 and the microcurrent unit 130 ( 120f) is formed.
  • 3 to 5 illustrate a microcurrent stimulating sock 100b according to a third embodiment of the present invention.
  • the microcurrent stimulation socks 100b according to the third embodiment of the present invention includes the first and second microcurrent stimulation parts 131 and 132 formed on the sole side of the socks,
  • the base 110 is formed of a general yarn, and a microcurrent generator 150.
  • the first and second microcurrent stimulation parts 131 and 132 are formed spaced apart at a predetermined interval on the sole side of the sock, and the first and second connection parts are provided on the first and second microcurrent stimulation parts 131 and 132, respectively. 161 and 162 are electrically connected.
  • the first and second microcurrent magnetic pole parts 131 and 132 and the first and second connection parts 161 and 162 are formed of a conductive yarn having good conductivity as in the previous embodiment.
  • the pocket part 200 is formed on the upper side of the sock, and the receiving space 210 in which the microcurrent generator 150 is accommodated is formed inside the pocket part 200.
  • a pair of first connection terminals 171 and 172 are connected to the microcurrent generator 150 through power lines 150a and 150b, and the first connection terminals 171 and 172 are made of a conductive material.
  • the one connecting terminal 171, 172 is formed in the groove shape.
  • the first and second connection parts 161 and 162 extend toward the pocket part 200, and a pair of second connection terminals 221 and 222 are formed on one side of the pocket part 200, and the second connection terminal (
  • the 221 and 222 are made of a conductive material and configured to be individually connected to the first and second connection portions 161 and 162.
  • Each of the second connection terminals 221 and 222 is formed in a protrusion shape.
  • the microcurrent generator 150 is accommodated in the accommodation space 210 of the pocket 200, and the first connection terminals 171 and 172 of the microcurrent generator 150 extend toward the pocket 200. It is electrically connected to the 2nd connection terminal 221,222 side.
  • the cover portion 230 is formed on the upper side of the pocket portion 200 to be opened and closed, and coupling means such as Velcro fasteners and snap buttons on the inner side of the cover portion 230 and one side of the pocket portion 200. 242 is provided, the cover portion 230 is coupled to the pocket portion 200 by the coupling means (241, 242) can maintain its closed state.
  • FIG. 6 illustrates a microcurrent stimulating sock 100c according to a fourth embodiment of the present invention.
  • a pair of first connection terminals 173 and 174 are formed in a protrusion shape on one side of the microcurrent generator 150 and a pair of second connections formed on the pocket part 200 side.
  • the terminals 223 and 224 are formed in a groove shape. Accordingly, the microcurrent generator 150 is accommodated in the accommodation space 210 of the pocket part 200, and the first connection terminals 173 and 174 of the microcurrent generator 150 extend toward the pocket part 200. It is electrically connected to the connection terminals 223 and 224 side.
  • FIG. 7 illustrates a microcurrent stimulating sock 100d according to a fifth embodiment of the present invention.
  • a pair of first connection terminals 175 and 176 are formed in a protrusion shape on one side of the microcurrent generator 150 and a pair of second connections formed on the pocket part 200 side.
  • the terminals 225 and 226 are formed in a projection shape. Accordingly, the microcurrent generator 150 is accommodated in the accommodation space 210 of the pocket part 200, and the second connection terminals 175 and 176 of the microcurrent generator 150 extend toward the pocket part 200. It is electrically connected to the connection terminals 225 and 226 side.
  • one side of the microcurrent generator 150 is attached to the coupling means 250, such as a clip or tongs, the microcurrent generator 150 by the coupling means 250 can be coupled to the pocket portion 200 side. have.
  • FIG 8 shows a circuit diagram according to a first embodiment of the microcurrent generator 150 used in the present invention.
  • the microcurrent generator 150 includes a power supply unit 152, a frequency generator 156, a control chip 157, and a generation current level control unit 158.
  • the generation voltage level control unit 154 for controlling the level of the generated voltage generated by the control chip 157 to the final voltage required for the human body may be further provided.
  • the generated voltage level controller 154 has a wiring structure shown in FIG. 8 including a resistor R3, a capacitor C1, and an inductor L. Referring to FIG. 8
  • the power supply unit 152 is connected to a battery for supplying power to the microcurrent generator 150.
  • the power supply unit 152 may include a battery for supplying power, a power switch S / W1 for determining whether the power is supplied to the microcurrent generator 150, and a battery level indicator D1 indicating the remaining amount of the battery. ) And battery indicator indicator switch (S / W2). At this time, the power switch (S / W1), the remaining battery indicator (D1), the remaining battery indicator indicator switch (S / W2) is exposed to the outside of the case for the user's operation and convenience, open for the user's battery replacement Closed lid is provided.
  • the power switch (S / W1) may be in a form that can be directly operated by the user, and also, if necessary, using a film switch, a resistance switch, a thermal switch, a touch switch, and the like, automatically and manually as needed. It is also possible to configure it to turn on and off.
  • the power supply unit 152 operates the microcurrent generator 150 only when the power switch S / W1 connected to the input terminal VIN of the control chip 157 is on to minimize battery consumption.
  • the battery power remaining indicator (D1) is connected to the LED control unit (LED) in the control chip 157, it is possible to turn on the LED lamp for each color such as red, blue, yellow so that the user can know.
  • the battery power indicator indicator switch (S / W2) is attached so that the user can specify whether the LED is on or off.
  • the brightness of the LED In addition, through the diode (D1) and the resistor (R4) connected to the LED control terminal (LED) of the control chip 157, the brightness of the LED, the interval of lighting (in seconds), the lighting time (in seconds or milliseconds) Adjust to minimize battery drain.
  • batteries all the batteries known to those skilled in the art may be used as the batteries. That is, all batteries can be used, including primary batteries such as alkaline batteries and manganese batteries, and secondary batteries such as lithium-ion, nickel-hydrogen and nickel-cadmium batteries.
  • primary batteries such as alkaline batteries and manganese batteries
  • secondary batteries such as lithium-ion, nickel-hydrogen and nickel-cadmium batteries.
  • battery power 3V coin battery as well as 1.5V general battery can be arranged in series to supply 3 ⁇ 12V DC power.
  • the frequency generator 156 is for controlling the generation cycle of the microcurrent generated through the microcurrent generator 150, by connecting a frequency crystal CRYSTAL to the Xin and Xout terminals of the control chip 157. Configure. Using the frequency generated by the frequency generator 156, the control chip 157 or the microcurrent generator 150 outputs a microcurrent at a desired time interval (seconds or milliseconds), and the enable terminal ( EN) to maintain the output for the desired time (in seconds or milliseconds).
  • the control chip 157 generates the microcurrent using the power supplied through the power supply unit 152, and controls the generation period of the microcurrent using the frequency generated by the frequency generator 156.
  • the generation time of the microcurrent is controlled in response to the enable signal input through the enable terminal EN from the outside.
  • the control chip 157 is configured to generate a microcurrent having the required voltage and current by using the power supplied from the battery of the power supply unit 152, the microcurrent generation cycle, the fine using the power supplied from the battery It converts a microcurrent with a current holding time, voltage and current of the required size.
  • the control chip 157 converts the power of the 2.5V ⁇ 12V voltage input through the battery into a voltage of 9V ⁇ 50V and a microcurrent of 1,000 kHz or less to supply a microcurrent beneficial to the human body.
  • the generation current level control unit 158 is to adjust the micro current generated by the control chip 157 to a desired level, and has a wiring structure as shown in FIG. 3 (R1, R2) and a variable resistor. (VR), condenser (C2), diode (D2), and transistor (TR1), through the microcurrent output from the control chip 157 to convert to a microcurrent of several hundreds to hundreds of microwatts to deliver to the human body do.
  • VR variable resistor
  • the overall operation of the microcurrent generator 150 is as follows.
  • the input power is amplified from 9V to 50V in the circuit in the control chip 157 and output to the outside of the control chip.
  • the amplified 9V to 50V voltage is output to the outside of the control chip 157 through the SW terminal SW in the control chip as the output voltage of the control chip 157.
  • the output voltage is readjusted to the final voltage required by the human body through the resistor R3, the capacitor C1, and the inductor L present in the generated voltage level controller 154 that is external to the control chip 157. .
  • the microcurrent output from the control chip 157 is output to the outside of the control chip 157 with a microcurrent size of at most 1,000 mA or less through the VSW terminal VSW of the control chip 157 as necessary.
  • the microcurrent is provided in the generation current level control unit 158, and is connected to the output terminals of the microcurrent generator 150, resistors R1 and R2, variable resistors VR, capacitors C2, and diodes D2.
  • the final output is adjusted to the current of the desired size.
  • the control chip 157 the original DC current only has a positive phase in nature, it has a function to alternately output a positive phase and a negative phase through the transistor (TR1).
  • the feedback (FB) of the control chip serves as a feedback function to check the accuracy of the final output.
  • the microcurrent generator 150 includes a control unit 310, a boosting unit 320, and a microcurrent output unit 330.
  • the control unit 310 is a first control signal (S1) for generating a fine current having a positive phase, a second control signal (S2) for generating a fine current having a negative phase, and for boosting the power supply voltage
  • the third control signal S3 is generated to control the generation of the microcurrent.
  • the control unit 310 checks the level of the microcurrent supplied to the human body through the microcurrent generator 150 and controls the third control signal S3 when the level is not a predetermined level, thereby increasing the voltage level of the boosted voltage. By varying the control the human body supply level of the microcurrent.
  • the control unit 310 may include a control chip having a CPU to generate the first to third control signals S1, S2, and S3.
  • the booster 320 boosts the power voltages Vdd and Vcc to a boosted voltage of a predetermined level in response to the third control signal S3 of the control unit 310 to the microcurrent output unit 330. Supply.
  • the booster circuit constituting the booster unit 320 includes a booster circuit of a DC-DC converter type using a back electromotive force of an inductor, a charge pump circuit using a capacitor, and to those skilled in the art.
  • Various well known boost circuits can be used.
  • the microcurrent output unit 330 generates a microcurrent of a desired level based on the boosted voltage boosted by the booster 320 and supplies the microcurrent to the specific site of the human body through contact terminals in contact with the human body. .
  • the microcurrent output unit 330 supplies the microcurrent having a positive phase when the first control signal S1 is input, and a negative phase when the second control signal S2 is input. Supply the microcurrent having a.
  • the microcurrent is a current level of 0-1500 mA (not including 0) and refers to the micro current in microamps.
  • the microcurrent output unit 330 is generated by selecting any current level that is determined to have the highest therapeutic effect or massage effect among current levels of 0 to 1500 mA (not including 0). For example, a microcurrent of 0 to 300 mA or a micro current of 150 to 150 mA can be output.
  • the microcurrent output unit 330 includes at least one voltage distribution circuit and a plurality of switching elements, and each of the plurality of switching elements may include the first control signal S1 or the first control element.
  • the switching operation may be performed in response to the two control signal S2.
  • the microcurrent can be varied in response to the skin resistance of the human body used to make the level of the microcurrent actually supplied to the human body constant.
  • the microcurrent output unit 330 generates a supply level confirmation signal for confirming the human body supply level of the microcurrent supplied to the human body and provides it to the control unit 310, and the control unit 310 provides the In response to the supply level confirmation signal, the level of the boosted voltage of the booster 320 is controlled.
  • the supply level confirmation signal in addition to the function of confirming the level of the microcurrent actually supplied to the human body also provides a function of confirming whether the conditions for the actual contact with the human body has been established.
  • FIG. 10 is a circuit diagram illustrating an example of implementation of the microcurrent generator of FIG. 9.
  • control unit 310a is a control chip (for example, PIC16F716) (U2), resistor (R4), capacitor (C4), power (Vcc), LED to determine whether the power supply ( Including the D2) has a wiring structure as shown in FIG.
  • the control chip U2 may be a generator of a control signal having various kinds of frequencies.
  • control unit 310a may include a first control signal S1 for generating a microcurrent having a positive phase, a second control signal S2 for generating a microcurrent having a negative phase, And generating a third control signal S3 for boosting the power voltage to control the microcurrent generation.
  • control unit 310a receives the supply level confirmation signal MC for confirming the human body supply level of the microcurrent supplied to the human body provided by the microcurrent output unit 330a to receive the booster 320a.
  • the level of the boosted voltage VC can be controlled.
  • the level control of the boosted voltage VC is possible through the third control signal.
  • control unit 310a checks the human body supply level of the microcurrent through the supply level confirmation signal MC, it is also possible to check whether the human body contact terminals P1 and P2 actually contact the human body. . This is because it is possible to determine that the human body contact terminals P1 and P2 are in contact with the human body if the supply level confirmation signal MC is within a certain range corresponding to the skin resistance because the range of the human body's skin resistance is determined. .
  • the control unit 310a first checks whether the human body contact terminals P1 and P2 are in contact with the human body through the supply level confirmation signal MC, and whether a microcurrent is generated. It is decided. That is, when it is confirmed that the human body is contacted through the supply level confirmation signal MC, the microcurrent generation is performed through the microcurrent generator, and then the function of confirming the actual human supply level of the microcurrent is performed. .
  • the power supply voltage may be configured to be supplied through a battery.
  • the booster 320a may include a switching element Q7, which is repeatedly switched by the third control signal S3 generated by the control unit 310a, an inductor L1, rectification and ripple prevention, and boost voltage.
  • a diode D1 for storage, capacitors C1 and C2, and a resistor R10 have a wiring structure as shown in FIG. 10.
  • a transistor is used as the switching element Q7, but various switching elements including a MOSFET may be used.
  • the boosting unit 320a may be configured through a DC-DC converter type boosting circuit including the boosting stage 10 in multiple stages, and may include various boosting circuits such as a boosting circuit. It is possible to implement
  • the microcurrent output unit 330a includes a plurality of voltage dividers using a plurality of resistors R1, R6, R2, R7, R8, and R9 and a plurality of switching elements Q1, Q2, Q3, Q4, Q5, and Q6. ) To output the microcurrent to the human body contact terminals (P1, P2).
  • the plurality of switching elements Q1, Q2, Q3, Q4, Q5, and Q6 use transistors, but various switching elements including MOSFETs may be applied.
  • Some switching elements Q6 and Q3 of the switching elements Q1, Q2, Q3, Q4, Q5 and Q6 are controlled by the first control signal S1 and some switching elements Q5 and Q4. Is controlled by the second control signal S2, and the remaining switching elements Q1 and Q2 are controlled by the voltage of the first node n1, that is, the boosted voltage VC.
  • the human body contact terminals P1 and P2 are mounted on specific parts of the human body (sites requiring treatment or massage), and the second human body contacts the microcurrent applied through the first human contact terminal P1 through the human body. It may be configured to return to the terminal (P2), or to allow the micro-current applied through the second human contact terminal (P2) to pass through the human body to return to the first human contact terminal (P1).
  • FIG. 11 is a timing diagram of the control signal and the fine current of FIG. 10.
  • the microcurrent generator 150 operates while the human body contact terminals P1 and P2 of the microcurrent generator 330a of the microcurrent generator 150 are mounted on a specific part of the human body.
  • control unit 310a When power is supplied through a battery, the control unit 310a generates a signal for confirming whether the human body is in contact with the microcurrent output unit 330a or the third control signal S3 for generating a general microcurrent. In addition, the supply level confirmation signal MC is received to check whether the human body contact terminals P1 and P2 actually touch the human body.
  • control unit 110a supplies the third control signal S3 for generating a microcurrent to the boosting unit 320a.
  • the third control signal S3 is a control signal whose width and period are adjusted for boosting.
  • the control unit 310a supplies the third control signal S3 to the boosting unit 320a.
  • the third control signal S3 is a control signal whose width and period are adjusted for boosting.
  • the switching element Q7 of the boosting unit 320a is turned on / off in response to the third control signal S3.
  • a forward bias is applied to the diode D2, and the capacitor C2 stores a voltage output through the diode D2, and the output voltage, that is, the boost voltage VC Eliminate pulsations (ripples).
  • the first node n1 Generates a boosted voltage VC several times to several ten times higher than the power supply voltages Vcc and Vdd. For example, assuming that the power supply voltage is 3V, it is possible to obtain a voltage of 30V. Of course, it is also possible to generate higher levels of voltage.
  • the switching element Q7 when the switching element Q7 repeatedly performs the on / off operation according to the width and the period of the third control signal S3 of the control unit 310a, the boosted voltage VC has a desired level. .
  • the control unit 310a When the boosted voltage VC reaches a desired level, the control unit 310a generates a first control signal S1 and a second control signal S2.
  • the first control signal S1 and the second control signal S2 may be generated at the same time as the supply of the power supply voltage of the control unit 310a, but it does not mean that the boosted voltage VC reaches a desired level. Therefore, it is assumed here that it occurs when the boosted voltage VC reaches a desired level.
  • the first control signal S1 is for generating a micro current having a positive phase
  • the second control signal S2 is for generating a micro current having a negative phase.
  • the first control signal S1 is shown in FIG. 11. It may have a waveform structure of the pulse (pulse) having a certain period and a certain duty ratio (duty ratio). For example, it may have a waveform structure having a period of 1 second and a constant voltage level for a time of 150 ms, and a voltage level of 0 for the remaining time.
  • the period or duty ratio may be changed by a unit of time, and the period or duty ratio may have a different waveform structure.
  • the second control signal S2 may have a waveform structure in the form of a pulse having a certain period and a constant duty ratio in a form having a predetermined phase difference from the first control signal S1.
  • the second control signal S2 has the same shape except that it has a predetermined phase difference from the first control signal S1.
  • the second control signal S2 should have a voltage level of 0 in a time interval t1 in which the first control signal S1 has a constant voltage level, and the first control signal S1 has a voltage of 0.
  • the waveform structure has a constant voltage level.
  • the pulse of the first control signal S1 and the pulse of the second control signal S2 are generated so as not to overlap. That is, the timing at which the switching elements Q6 and Q3 are turned on by the first control signal S1 and the timing at which the switching elements Q5 and Q4 are turned on by the second control signal S2 should be different. Immediately after the switching elements Q6 and Q3 are turned on by the first control signal S1 and turned off again, the switching elements Q5 and Q4 are turned on by the second control signal S2. Also, the switching elements Q6 and Q3 are turned on by the first control signal S1 and then turned off again, and after a predetermined time, the switching elements Q5 and Q4 are turned on by the second control signal S2. It is also possible to turn on. This is possible by controlling the timing of the pulse generation of the second control signal S2, and may be determined differently as necessary in consideration of treatment or massage effects.
  • the microcurrent output unit 330a turns on the switching element Q1 by the voltage divided by the voltage distribution of the resistors R1 and R6.
  • the voltage divided by the voltage distribution of R2 and R7 turns on the switching element Q2. This is possible when the switching elements Q5 and Q6 are turned off.
  • the switching element Q6 is turned on by the first control signal S1 even when the boost voltage VC reaches a predetermined level.
  • the switching device Q2 is turned on and the switching device Q1 is turned off, and the switching device Q5 is turned on by the second control signal S2, the switching device Q1 is turned on and switched. Element Q2 is turned off.
  • the switching device Q2 When the switching devices Q6 and Q3 are turned on by the first control signal S1 and the switching devices Q5 and Q4 are turned off by the second control signal S2, the switching device Q2. ) Is turned on, and the microcurrent is supplied to the human body through the switching element Q2 and the human body contact terminal P1 at the first node n1, and the microcurrent supplied to the human body is the human body contact terminal P2 and It is recovered through the switching element Q3 and the resistors R8 and R9. At this time, the switching elements Q5, Q4, and Q1 are turned off by the second control signal S2. At this time, the microcurrent supplied to the human body has a positive phase, as shown in the microcurrent graphs P1-P2 of FIG. 11.
  • the switching devices Q6 and Q3 are turned off by the first control signal S1 and the switching devices Q5 and Q4 are turned on by the second control signal S2, the switching device Q1.
  • the microcurrent is supplied to the human body through the switching element Q1 and the human body contact terminal P2 at the first node, and the microcurrent supplied to the human body is the human body contact terminal P1 and the switching element ( Q4), it is recovered through the resistors R8 and R9.
  • the switching elements Q6, Q3, and Q2 are turned off by the first control signal S2.
  • the microcurrent supplied to the human body has a negative phase, as shown in the microcurrent graphs P1-P2 of FIG. 11.
  • the level of microcurrent supplied to the human body is different for each human body because the skin resistance is different for each human body. Therefore, in order to increase the massage or treatment effect, since the microcurrent within a certain level range must be supplied, there is a need to check the level of the microcurrent actually supplied to the human body.
  • the microcurrent output unit 330a has a configuration capable of controlling the level of the microcurrent supplied to the human body by checking the level of the microcurrent recovered through the human body contact terminals P1 and P2.
  • the supply level confirmation signal MC may send a minute current flowing through the resistors R8 and R9 to the control unit 310a. As shown in FIG. 10, the voltage distribution of the resistors R8 and R9 may be divided. It is also possible to use the divided voltage level as the supply level confirmation signal MC.
  • the supply level confirmation signal MC is provided to the control chip U2 of the control unit 310a, and when the supply level confirmation signal MC is provided, the control unit 310a analyzes the supply level confirmation signal MC to the human body. It is confirmed whether the level of the microcurrent actually supplied is the desired level.
  • the boosting unit 320a is boosted through the third control signal S3.
  • the level of the voltage VC is controlled.
  • the level of the boosted voltage VC When the level of the boosted voltage VC is controlled, the level of the microcurrent actually supplied to the human body through the human body contact terminals P1 and P2 is changed, and the control through the control unit 310a is controlled by the human body. The level of microcurrent actually supplied is continued until the desired level range is reached.
  • microcurrent stimulation socks of the present invention it is very useful for the healing of damaged tissues by flowing a microcurrent to the damaged tissues such as pressure ulcers, congestive ulcers and diabetic ulcers.
  • the most direct effect of microcurrent stimulation is to reduce the stimulation of the sympathetic nerve, which causes the contraction of muscles located in the vessel wall in the peripheral blood vessels, thereby reducing blood flow, thereby increasing blood flow to the skin.
  • various studies have shown that the effect of microcurrent can increase tissue oxygen saturation with the increase of blood flow in diabetic ulcer sites.
  • microcurrent stimulation stimulates angiogenesis, increases the biosynthesis of fibroblasts and proteins, and the flow of current from the cathode to the anode increases the migration of fibroblasts and synthesized proteins in wound margins, preventing bacterial growth. It has an effect on wound healing with an increase in tissue oxygen saturation copper due to increased blood flow.
  • the angiogenic stimulating effect of the microcurrent is caused by the increased production of VEGF by the current.
  • Microcurrent during electrostimulation therapy is also called “biological stimulation” or “bioengineering” because of its ability to stimulate cell physiology and growth.
  • Microcurrent has an excellent effect on wound healing, and one of the mechanisms of wound healing has been hypothesized to facilitate intracellular metabolism and stimulate ATP production by energizing the body with the same microcurrent. Since microcurrents have been found to directly affect local microcirculation to soothe inflammation, many studies have been conducted and the high effects of microcurrents on the treatment and wound healing of Achilles tendonitis have been reported in several papers. In addition, since the microcurrent is carried out in a range below the sensory sense almost no current has the advantage that can be treated without the discomfort caused by the current appearing in the previous electrotherapy.
  • Percutaneous oxygen partial pressure measurement has been widely used as the most important method for determining the effects of electrostimulation therapy in diabetic foot disease patients.
  • Percutaneous oxygen partial pressure measurement is a non-invasive test method that can measure the skin micro blood flow and blood gas by measuring the absolute value of oxygen partial pressure in the epidermis and dermis.
  • Percutaneous oxygen partial pressure measurement is also an important indicator for predicting the risk of wound healing and amputation. If the percutaneous oxygen partial pressure measured at the wound is less than 20 mmHg, healing of the wound can hardly occur. After electrical stimulation treatment, sympathetic nerve stimulation is reduced, and peripheral blood vessel response causes vasodilation and an increase in capillaries at the electrical stimulation site, indicating an increase in percutaneous oxygen partial pressure. Many previous studies have shown that the percutaneous partial pressure of oxygen measured after electrostimulation has increased by an average of 14 mmHg, resulting in reduced amputation in diabetic foot disease patients.
  • the microcurrent stimulation therapy can be used for the control of pain in various musculoskeletal disorders and neurological diseases such as myofascial pain syndrome, tennis elbow, shoulder adhesive adhesions, arthritis, as well as peripheral neuropathy such as diabetic neuropathy and disc disease.
  • myofascial pain syndrome such as myofascial pain syndrome, tennis elbow, shoulder adhesive adhesions, arthritis, as well as peripheral neuropathy such as diabetic neuropathy and disc disease.
  • peripheral neuropathy such as diabetic neuropathy and disc disease.
  • Pain threshold can be lowered by promoting back secretion.
  • the present invention it is possible to generate a microcurrent through the microcurrent generator, to control the level of the generated microcurrent, and to deliver the microcurrent through the conduction yarn to treat the foot massage effect or diabetes. Can be more effectively achieved.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Biophysics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Electrotherapy Devices (AREA)
  • Socks And Pantyhose (AREA)
  • Finger-Pressure Massage (AREA)

Abstract

La présente invention concerne une chaussette destinée à être portée sur la région du pied à des fins thérapeutiques ou de massage et, plus particulièrement, une chaussette de stimulation par micro-courant qui stimule la région du pied par transmission d'un micro-courant de façon à renforcer les effets d'un massage, d'une thérapie, etc. La chaussette de stimulation par micro-courant selon la présente invention comprend : un ensemble de stimulation par micro-courant pourvu d'un fil conducteur sur au moins une partie de la chaussette ; un générateur de micro-courant, fixé à une certaine partie en haut de la région de la cheville, pour générer un micro-courant destiné à être appliqué au fil conducteur façonnant l'ensemble de stimulation par micro-courant, à certains intervalles, durant un temps de mise sous tension ; une partie de connexion, faite du même matériau que l'ensemble de stimulation par micro-courant, servant à relier électriquement l'ensemble de stimulation par micro-courant au générateur de micro-courant ; et une partie de base faite de fil classique pour constituer les parties restantes de la chaussette, autres que l'ensemble de stimulation par micro-courant et la partie de connexion.
PCT/KR2011/001342 2010-03-26 2011-02-25 Chaussette de stimulation par micro-courant Ceased WO2011118918A2 (fr)

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Cited By (6)

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DE102014018683A1 (de) 2014-12-18 2016-06-23 miha bodytec GmbH EMS-Reizstromübertragungselement, sowie mit dem EMS-Reizstromübertragungselement ausgestattetes EMS-Kleidungsstück
JP2017159091A (ja) * 2017-05-12 2017-09-14 日立マクセル株式会社 マッサージ装置
EP3305362A3 (fr) * 2016-10-06 2018-08-01 StimMed LLC Procédé et appareil d'inhibition non invasive de la thrombose veineuse profonde
US10213593B2 (en) 2010-01-15 2019-02-26 Stimmed Llc Method and apparatus for noninvasive inhibition of deep vein thrombosis
US10300271B2 (en) 2014-12-16 2019-05-28 miha bodytec GmbH EMS training device, and method for protecting an EMS training device
US10835736B2 (en) 2014-09-05 2020-11-17 miha bodytec GmbH EMS exercise device, EMS electrode, EMS garment, EMS stimulus generating unit, EMS signal cable, and EMS undergarment for an EMS exercise device, and method for operating the EMS exercise device

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FR2833497B1 (fr) * 2001-12-17 2004-11-19 Innothera Topic Int Article tricote therapeutique de type bas, chaussette ou collant pour le traitement par electromyostimulation des troubles fonctionnels de l'insuffisance veineuse des membres inferieurs
KR200325057Y1 (ko) * 2003-05-27 2003-09-02 노광균 물품보관용 포켓이 있는 양말
KR200351588Y1 (ko) * 2004-02-23 2004-05-27 류수현 군용 동상방지 양말
JP2005245909A (ja) * 2004-03-08 2005-09-15 Soeki Yu 電気刺激マッサージおおい
JP2008539051A (ja) * 2005-04-28 2008-11-13 キャロル コール カンパニー マイクロダーマルトーン皮膚刺激装置
KR100685445B1 (ko) * 2006-02-09 2007-02-26 김병수 비염치료기

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10213593B2 (en) 2010-01-15 2019-02-26 Stimmed Llc Method and apparatus for noninvasive inhibition of deep vein thrombosis
US10835736B2 (en) 2014-09-05 2020-11-17 miha bodytec GmbH EMS exercise device, EMS electrode, EMS garment, EMS stimulus generating unit, EMS signal cable, and EMS undergarment for an EMS exercise device, and method for operating the EMS exercise device
US10300271B2 (en) 2014-12-16 2019-05-28 miha bodytec GmbH EMS training device, and method for protecting an EMS training device
DE102014018683A1 (de) 2014-12-18 2016-06-23 miha bodytec GmbH EMS-Reizstromübertragungselement, sowie mit dem EMS-Reizstromübertragungselement ausgestattetes EMS-Kleidungsstück
US10814123B2 (en) 2014-12-18 2020-10-27 miha bodytec GmbH EMS stimulation current transmission element and EMS garment equipped with the EMS stimulation current transmission element
EP3305362A3 (fr) * 2016-10-06 2018-08-01 StimMed LLC Procédé et appareil d'inhibition non invasive de la thrombose veineuse profonde
JP2017159091A (ja) * 2017-05-12 2017-09-14 日立マクセル株式会社 マッサージ装置

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